Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.
- NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_assertion description "[A null mutation in this protein was evaluated for a relationship to disease susceptibility and disease severity in patients with multiple sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.
- NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_assertion evidence source_evidence_literature NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.
- NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_assertion SIO_000772 11857064 NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.
- NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_assertion wasDerivedFrom lhgdn-20090331 NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.
- NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_assertion wasGeneratedBy ECO_0000203 NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP193358.RAdRQaL31hkrm3XsrLJ9rFv22uKI6U7NVnthuNXa_PWuc130_provenance.